Identity
- Trade Name
- AnkleTough® FDA UDI
- Generic Name
- Body/limb elastic exerciser FDA UDI
- Device Name
- AnkleTough® rehab system of tension straps and exercises designed as an aid to rehabilitate and strengthen injured ankles; most commonly sprained ankles, 4-Strap Set (1-Strap Each Level - Light, Medium, Strong, and Tough) FDA UDI
- Model / Reference
- 20831727009809 FDA UDI
- Description
- AnkleTough® rehab system of tension straps and exercises designed as an aid to rehabilitate and strengthen injured ankles; most commonly sprained ankles, 4-Strap Set (1-Strap Each Level - Light, Medium, Strong, and Tough) FDA UDI
Identifiers
- Catalog Number
- 20831727009809 FDA UDI
- Primary DI / UDI-DI
- G064208317270098090 FDA UDI
- FDA Product Code
- IOD FDA UDI
- GMDN Term
- Body/limb elastic exerciser FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5350 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
AnkleTough® by Walgreen Health Solutions, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Walgreen Health Solutions, LLC
Sources (1)
- FDA UDI fd859ccd-dee8-4bc8-9894-7a8c6fce10e9 36 fields · synced Jun 8, 2026